42 SEMEN FERTILITY OF THE BULL EVALUATED BY SECOND-ORDER STATISTICS

2010 ◽  
Vol 22 (1) ◽  
pp. 178
Author(s):  
T. F. Silva ◽  
J. B. Barreto Filho ◽  
R. S. Macedo ◽  
M. V. C. Ferraz Jr ◽  
R. A. Braga Jr ◽  
...  

The biospeckle (BSL) is based on the incidence of laser light upon active biological materials, followed by analysis and manipulation of secondary images, and then, application to those images of a second-order statistics technique called the inertial moment (IM) that results in information about the activity of the specimen. This technique was previously used to analyze sperm motility. A bull’s fertility could be evaluated by several semen parameters in vitro and more precisely by conception rates of AI heifers. The objective of this work was to evaluate the fertility of bull’s frozen semen showing different levels of activity in an AI program. Semen of 6 mature IA donor bulls (Bos taurus indicus) was previously divided in 2 groups (group I: motility ≥50%; group II: motility <50%), each group comprising 3 animals. Sperm concentration was 30 to 35 × 106 cells per straw. Semen was thawed at 37°C for 30 s in a water bath. Samples were illuminated by nonpolarized He-Ne laser (632 nm, 10 mW) for 40 s, the time needed to take 512 images under a time rate of 0.08 s. Images were acquired by a CCD camera and analyses were conducted by building space-time speckle matrices from center columns of 512 images of the dynamic speckle and then the IM was calculated. Beef heifers (n = 109) under the same nutrition and management conditions underwent AI with the semen samples. All inseminations were done by the same technician and donor bulls were used consecutively throughout the breeding season. Pregnancy diagnosis was done by ultrasound images (Falco 100, 6 MHz, Pie Medical, Crawley, UK) 28 days after insemination. The SISVAR software was used for variance analysis and comparison of means by Tukey test at a nominal level of 5%. The IM (194.13 ± 31.99) obtained from 10 illuminations per sample of each bull and the conception rate (CR) of group I (CR = 0.63 ± 0.49) differed (P < 0.05) compared with group II (IM = 142.03 ± 30.62; CR = 0.43 ± 0.50). Pearson correlation coefficient (P < 0.05) between IM and CR was r = 0.21, showing coherence with IM and CR, despite its low value. These data showed that second-order statistics are correlated to semen fertility and could be used to evaluate ejaculates of the bull. Financial support: FAPEMIG grant EDT 94/07 and CNPq.

2003 ◽  
Vol 52-54 ◽  
pp. 467-472 ◽  
Author(s):  
Hauke Bartsch ◽  
Klaus Obermayer

2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Kang-Sheng Liu ◽  
Xiao-Dong Mao ◽  
Feng Pan ◽  
Rui Fang An

AbstractRecent years have seen a rising incidence of male infertility, mostly caused by the decline of sperm quality. The ratio of infertile males to infertile females has escalated from 3:7 in 2013 to current 5:5, which turns male infertility into the research focus of reproductive medicine. This study aimed to clarify the effect of reproductive tract infection by ureaplasma urealyticum (UU) and chlamydia trachomatis (CT) on the DNA integrity and routine semen parameters of infertile males. A retrospective study was performed. A total of 259 infertile males who were treated at the Andrological Laboratory Examination and Reproductive Medicine Center in our hospital were analyzed. qRT-PCR was used to examine the infection status of CT and UU. According to the eligibility criteria, we evaluated the semen parameters and biochemical data of 253 men. Based on the results of PCR, the subjects were divided into four groups: Group I (CT positive, 63 cases), Group II (UU positive, 60 cases), Group III (CT positive and UU positive, 62 cases), and Group IV (no infection, 68 cases). DNA fragmentation index (DFI), sperm count, vitality and morphology, elastase level, seminal plasma malondialdehyde (MDA), and total antioxidant capacity (TAC) were assessed. Compared to Group IV, three groups (Group I, Group II and Group III) showed difference in semen volume, proportion of sperm with normal morphology, sperm motility, progressive motility, and vitality (P < 0.05). Compared to Group IV, Group II and Group III showed difference in DFI (P < 0.05). Compared to Group IV, Group II and Group III showed difference in elastase level (P < 0.05). VCL, VSL, VAP, WOB, ROS, TM, HDS showed differences between groups of abnormal/normal WBC (*P < 0.01).UU infection significantly increased the level of seminal leukocytes only in Group II, but not in the other three groups, indicating that UU is a factor to increase the level of seminal leukocytes. Compared with the normal leukocyte group, there were significant differences in total motility, forward motility and normal sperm ratio between the two groups. The proportion of sperm with abnormal morphology (mostly in the head) showed obvious difference between groups of high and normal seminal leukocytic levels. At the same time, in this study, SCGE and SCD verified that leukocytes could damage sperm DNA by increasing ROS, which ultimately affects male fertility.


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